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Interleukin-2 Gene Expression in Central Nervous system Cells after Stress and Antigen Application. / Korneva, E.A.; Kazakova, T.B.

NeuroImmune Biology : Cytokines and the Brain. Том 6 Elsevier, 2007. стр. 353-372.

Результаты исследований: Публикации в книгах, отчётах, сборниках, трудах конференцийглава/раздел

Harvard

Korneva, EA & Kazakova, TB 2007, Interleukin-2 Gene Expression in Central Nervous system Cells after Stress and Antigen Application. в NeuroImmune Biology : Cytokines and the Brain. Том. 6, Elsevier, стр. 353-372. https://doi.org/10.1016/S1567-7443(07)10017-X

APA

Korneva, E. A., & Kazakova, T. B. (2007). Interleukin-2 Gene Expression in Central Nervous system Cells after Stress and Antigen Application. в NeuroImmune Biology : Cytokines and the Brain (Том 6, стр. 353-372). Elsevier. https://doi.org/10.1016/S1567-7443(07)10017-X

Vancouver

Korneva EA, Kazakova TB. Interleukin-2 Gene Expression in Central Nervous system Cells after Stress and Antigen Application. в NeuroImmune Biology : Cytokines and the Brain. Том 6. Elsevier. 2007. стр. 353-372 https://doi.org/10.1016/S1567-7443(07)10017-X

Author

Korneva, E.A. ; Kazakova, T.B. / Interleukin-2 Gene Expression in Central Nervous system Cells after Stress and Antigen Application. NeuroImmune Biology : Cytokines and the Brain. Том 6 Elsevier, 2007. стр. 353-372

BibTeX

@inbook{7ab69f8e5faf43f18f04e978bc0dc977,
title = "Interleukin-2 Gene Expression in Central Nervous system Cells after Stress and Antigen Application",
abstract = "In this article we summarize the data concerning the expression of immediate early gene (IEG), c-fos, in brain cells, which encodes for one of the interleukin-2 (IL-2) cytokine transcriptional factors. The main molecular features and tissue-specific differences of IL-2 and IL-2 receptors in the brain are also discussed. Various forms of stress stimulated the expression of c-fos and IL-2 genes in central nervous system (CNS) neurons has been shown after different stressor stimuli. Stress activated IEG expression in cells of definite hypothalamic structures.Antigen injection led to the activation of c-fos and IL-2 gene expression specifically in the cells of definite hypothalamic nuclei and in other areas of rat brain. A temporospatial pattern of activation of hypothalamic structures was found consistently in response to exposure to antigen, which was different from that induced by other stressors.Short synthetic immunomodulating peptides influenced IEG expression in immune and nervous system cells. Definite physical factors, like Extremely high-frequency electromagnetic millimeter waves (EHF) skin irradiation, modulated (mostly decreased) the stress-induced stimulation of IEG genes in hypothalamic neurons. We discuss the possible role of the JAK-STAT and Ras-MAPK signal transduction pathways in IL-2 gene expression in lymphocytes and in nerve cells.",
author = "E.A. Korneva and T.B. Kazakova",
year = "2007",
doi = "https://doi.org/10.1016/S1567-7443(07)10017-X",
language = "English",
isbn = "044453041X",
volume = "6",
pages = "353--372",
booktitle = "NeuroImmune Biology",
publisher = "Elsevier",
address = "Netherlands",

}

RIS

TY - CHAP

T1 - Interleukin-2 Gene Expression in Central Nervous system Cells after Stress and Antigen Application

AU - Korneva, E.A.

AU - Kazakova, T.B.

PY - 2007

Y1 - 2007

N2 - In this article we summarize the data concerning the expression of immediate early gene (IEG), c-fos, in brain cells, which encodes for one of the interleukin-2 (IL-2) cytokine transcriptional factors. The main molecular features and tissue-specific differences of IL-2 and IL-2 receptors in the brain are also discussed. Various forms of stress stimulated the expression of c-fos and IL-2 genes in central nervous system (CNS) neurons has been shown after different stressor stimuli. Stress activated IEG expression in cells of definite hypothalamic structures.Antigen injection led to the activation of c-fos and IL-2 gene expression specifically in the cells of definite hypothalamic nuclei and in other areas of rat brain. A temporospatial pattern of activation of hypothalamic structures was found consistently in response to exposure to antigen, which was different from that induced by other stressors.Short synthetic immunomodulating peptides influenced IEG expression in immune and nervous system cells. Definite physical factors, like Extremely high-frequency electromagnetic millimeter waves (EHF) skin irradiation, modulated (mostly decreased) the stress-induced stimulation of IEG genes in hypothalamic neurons. We discuss the possible role of the JAK-STAT and Ras-MAPK signal transduction pathways in IL-2 gene expression in lymphocytes and in nerve cells.

AB - In this article we summarize the data concerning the expression of immediate early gene (IEG), c-fos, in brain cells, which encodes for one of the interleukin-2 (IL-2) cytokine transcriptional factors. The main molecular features and tissue-specific differences of IL-2 and IL-2 receptors in the brain are also discussed. Various forms of stress stimulated the expression of c-fos and IL-2 genes in central nervous system (CNS) neurons has been shown after different stressor stimuli. Stress activated IEG expression in cells of definite hypothalamic structures.Antigen injection led to the activation of c-fos and IL-2 gene expression specifically in the cells of definite hypothalamic nuclei and in other areas of rat brain. A temporospatial pattern of activation of hypothalamic structures was found consistently in response to exposure to antigen, which was different from that induced by other stressors.Short synthetic immunomodulating peptides influenced IEG expression in immune and nervous system cells. Definite physical factors, like Extremely high-frequency electromagnetic millimeter waves (EHF) skin irradiation, modulated (mostly decreased) the stress-induced stimulation of IEG genes in hypothalamic neurons. We discuss the possible role of the JAK-STAT and Ras-MAPK signal transduction pathways in IL-2 gene expression in lymphocytes and in nerve cells.

U2 - https://doi.org/10.1016/S1567-7443(07)10017-X

DO - https://doi.org/10.1016/S1567-7443(07)10017-X

M3 - Chapter

SN - 044453041X

VL - 6

SP - 353

EP - 372

BT - NeuroImmune Biology

PB - Elsevier

ER -

ID: 4454208